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Home/Diagnosis/ICD-10 Coding for Lipin-1 Deficiency

ICD-10 Coding for Lipin-1 Deficiency

E88.81
M62.82
R82.2

Complete ICD-10-CM coding and documentation guide for icd-10 coding for lipin-1 deficiency includes clinical validation requirements, medical necessity guidelines, and coding policies.

Also Known as:
LPIN1 Mutation
Recurrent Rhabdomyolysis due to Lipin-1 Deficiency
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Key Information: ICD-10 Coding for Lipin-1 Deficiency

Essential facts and insights about ICD-10 Coding for Lipin-1 Deficiency

Use ICD-10 code E88.81 for other specified metabolic disorders, ensuring proper documentation in clinical notes.

Primary ICD-10-CM Codes

Other specified metabolic disorders

Non-Billable
E88.81
Non-Billable

Diagnostic Criteria

  • • Confirmed LPIN1 mutation with recurrent rhabdomyolysis episodes.

Applicable To

  • • Lipin-1 deficiency

Important Notes

  • • Ensure genetic testing is documented to support E88.81.

Rhabdomyolysis

Billable Code
M62.82
Billable

Diagnostic Criteria

  • • CK levels >10,000 IU/L
  • • Muscle pain and swelling

Applicable To

  • • Acute rhabdomyolysis

Important Notes

  • • Ensure documentation of acute rhabdomyolysis episode.

Myoglobinuria

Billable Code
R82.2
Billable

Diagnostic Criteria

  • • Urine myoglobin >300 ng/mL

Applicable To

  • • Presence of myoglobin in urine

Important Notes

  • • Ensure urine test confirms myoglobin presence.
Ancillary Codes

Additional codes that may be used with this diagnosis

R82.2

Myoglobinuria

Use when myoglobinuria is present due to rhabdomyolysis.

Frequently Asked Questions

What is the ICD-10 code for Lipin-1 deficiency?

The ICD-10 code for Lipin-1 deficiency is E88.81, which is used for other specified metabolic disorders.

How is Lipin-1 deficiency diagnosed?

Lipin-1 deficiency is diagnosed through genetic testing confirming LPIN1 mutations, often accompanied by recurrent rhabdomyolysis episodes.

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